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Arrowhead Files for Regulatory Clearance to Begin Phase 1 Study of ARO-ANG3 [复制链接]

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发表于 2018-10-15 19:55 |只看该作者 |倒序浏览 |打印
Arrowhead Pharmaceuticals Files for Regulatory Clearance to Begin Phase 1 Study of ARO-ANG3
Oct 15, 2018 at 7:30 AM EDT
— Arrowhead to host R&D Day October 16, 2018 to discuss ARO-ANG3 and its emerging pipeline of RNAi therapeutics PASADENA, Calif. --(BUSINESS WIRE)--Oct. 15, 2018-- Arrowhead Pharmaceuticals Inc. (NASDAQ: ARWR) today announced that it has filed an application for approval to begin a Phase 1 clinical
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— Arrowhead to host R&D Day October 16, 2018 to discuss ARO-ANG3 and its emerging pipeline of RNAi therapeutics

PASADENA, Calif.--(BUSINESS WIRE)--Oct. 15, 2018-- Arrowhead Pharmaceuticals Inc. (NASDAQ: ARWR) today announced that it has filed an application for approval to begin a Phase 1 clinical trial of ARO-ANG3, an RNAi-based investigational medicine targeting angiopoietin like protein 3 (ANGPTL3) being developed for the treatment of dyslipidemias and metabolic diseases. ARO-ANG3 will be the fourth therapeutic candidate to enter clinical studies that leverages Arrowhead’s Targeted RNAi Molecule (TRiM™) platform.

Chris Anzalone, Ph.D., president and CEO of Arrowhead Pharmaceuticals, said: “The ARO-ANG3 program has moved rapidly through preclinical development and we are thrilled to now submit the regulatory filing ahead of schedule. After positive initial signs of tolerability and activity with ARO-AAT and ARO-HBV, our first two clinical programs leveraging the TRiM™ platform, we are moving into the ARO-ANG3 clinical program with confidence.”

Pending approval, Arrowhead intends to proceed with AROANG1001, a Phase 1 single and multiple dose study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamic effect of ARO-ANG3 in adult healthy volunteers and dyslipidemic patients. The study is designed to enroll up to 70 subjects.

An application was submitted to an ethics committee in compliance with the Clinical Trial Notification process of the Australian Department of Health and Ageing, Therapeutic Goods Administration.

As a reminder, Arrowhead will host a Research & Development (R&D) Day to discuss ARO-ANG3 and its emerging pipeline of RNAi therapeutics that leverage the Company’s proprietary Targeted RNAi Molecule (TRIM™) platform on October 16, 2018 in New York City.

The R&D Day will feature presentations by Ira Goldberg, M.D. (NYU Langone Medical Center), who will discuss the current treatment landscape and unmet medical need for patients with dyslipidemia and hypertriglyceridemia.

Arrowhead’s management team will provide an overview of the company’s pipeline of RNAi-based therapeutics. Discussion topics will include:

ARO-APOC3 for patients with hypertriglyceridemia. A CTA filing is planned by the end of 2018
ARO-ANG3 for patients with dyslipidemia
ARO-ENaC for patients with cystic fibrosis. A CTA filing is planned in 2019
ARO-HIF2 for patients with renal cell carcinoma. A CTA filing is planned in 2019
This event is intended for institutional investors, sell-side analysts, investment bankers, and business development professionals only. Please RSVP in advance if you plan to attend, as space is limited. To reserve a seat, please click here to register.

A live and archived webcast of the event, with slides, may be accessed on the Events and Presentations page under the Investors section of the Arrowhead website.

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发表于 2018-10-15 19:55 |只看该作者

2018年10月15日,在早上7:30
——箭头主持研发天2018年10月16日讨论ARO-ANG3及其新兴管道RNAi疗法帕萨迪纳,加利福尼亚州——(业务线)——10月。 2018——箭头制药有限公司(纳斯达克:ARWR)今天宣布,它已申请批准开始1期临床
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——箭头主持研发的一天2018年10月16日讨论ARO-ANG3及其 新兴的RNAi疗法

加州帕萨迪纳市。——(业务线)——10月。 15日,2018年,箭头制药公司。(纳斯达克:ARWR)今天宣布,它 已申请批准开始第一阶段临床试验 RNAi-based ARO-ANG3的试验性药物目标 检验像蛋白3(ANGPTL3)正在开发的治疗 血脂异常和代谢疾病。 ARO-ANG3将第四 利用治疗候选人进入临床研究 箭头的有针对性的RNAi分子(修剪™)平台。

克里斯Anzalone博士,总裁兼首席执行官箭头制药, 说:“ARO-ANG3程序已经通过临床前迅速 发展和我们现在激动提交监管申报文件中 比原计划提前。 经过积极的初步迹象的耐受性和 活动与ARO-AAT ARO-HBV,我们前两个临床项目 利用修剪™平台,我们正进入ARO-ANG3临床 计划有信心。”

等待批准,箭头打算继续AROANG1001,一个阶段 1单个和多个剂量研究来评估安全,耐受性, 药物动力学和药效学的影响ARO-ANG3成人 健康的志愿者和dyslipidemic患者。 这项研究的目的是 招收70名受试者。

应用程序提交伦理委员会符合 临床试验流程的通知澳大利亚 健康和老龄化,治疗商品管理。

提醒一下,箭头将主持研发(R&D)的一天 讨论ARO-ANG3及其新兴管道的RNAi疗法 利用公司的专有的有针对性的RNAi分子(修剪™) 平台2018年10月16日在纽约。

研发一天将功能演示爱尔兰共和军戈德堡医学博士(纽约大学 Langone医学中心),他将讨论当前的治疗 景观和血脂异常患者和未满足的医疗需求 高甘油三酯血症。

箭头的管理团队将提供该公司的概况 管道RNAi-based疗法。 讨论主题将包括:

ARO-APOC3高甘油三酯血症患者。 CTA的文件是 计划到2018年年底
ARO-ANG3血脂异常患者
ARO-ENaC囊性纤维化患者。 CTA申请计划 2019年
ARO-HIF2肾细胞癌患者。 CTA的文件是 2019年计划
这次活动的目的是为机构投资者,卖方分析师, 投资银行家和业务开发专家。 请 回复如果你提前计划参加,因为空间是有限的。 要预订 座位点击 在这里注册。

生活和归档事件的网络直播,幻灯片,可以访问 在事件 和演示页面下投资者的箭头 的网站。

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